NICE clinical guideline: antibiotics for the prevention and treatment of early-onset neonatal infection: Table 1

Author(s):  
Emma Caffrey Osvald ◽  
Philippa Prentice
Author(s):  
Siba Prosad Paul ◽  
Henna Khattak ◽  
Prashant Karkala Kini ◽  
Paul Anthony Heaton ◽  
Nitin Goel

2019 ◽  
Vol 62 (2) ◽  
pp. 58-61
Author(s):  
Štěpán Kutílek ◽  
Martina Vracovská ◽  
Kamila Pečenková ◽  
Hana Brožíková ◽  
Richard Pikner ◽  
...  

Introduction: Ionised hypocalcemia (S-Ca2+) has been repeatedly observed in neonates with sepsis. Our aim was to evaluate total calcemia (S-Ca) and its relationship to laboratory markers of infection. Methods: We retrospectively evaluated total calcemia (S-Ca) and its relationship to laboratory markers of sepsis/infection (serum levels of C-reactive protein – S-CRP and procalcitonin – S-PCT) in 29 full-term neonates with early-onset neonatal infection hospitalized at our neonatology ward between 2012 and 2016. The control group consisted of 705 neonates without infection. Results: In neonates with early-onset infection , the S-Ca on day 1, 2 and 3 was significantly lower (p < 0.0001; p < 0.0001; p = 0.05 versus controls) same as the pooled S-Ca (p < 0.0001 versus controls). There was a weak negative correlation between pooled S-Ca and S-PCT, or pooled S-Ca and S-CRP (r = −0.22, p = 0.06; r = −0.19, p = 0.09). Conclusion: S-Ca was decreased in neonates with early-onset infection and did show a slight tendency to inverse correlation with S-CRP and S-PCT. Pediatricians must be aware of the fact that a drop in total S-Ca should alert their attention to the risk of neonatal infection, and, likewise, that the children with neonatal infection are at a higher risk of hypocalcemia with all its consequences.


Author(s):  
Kirsty Le Doare ◽  
Christine E. Jones ◽  
Paul T. Heath

Group B Streptococcus (GBS) is a leading cause of early neonatal infection and neonatal mortality, with long-term adverse neurodevelopmental outcomes in up to 50% of survivors of GBS meningitis. GBS has a likely underappreciated role in causing preterm birth and stillbirth. GBS colonizes the vagina and gastrointestinal tract of the pregnant woman, and transmission to the infant occurs during or just before delivery. Although the majority of these infants do not develop invasive disease, maternal colonization is a prerequisite for early onset disease (0–6 days of life, most commonly associated with sepsis and respiratory distress) and a significant risk factor for late onset disease (7–89 days of life, most commonly associated with sepsis and meningitis). The introduction of intrapartum antibiotic prophylaxis has resulted in significant declines in the incidence of early onset disease but provides no protection against late onset disease.


2020 ◽  
Vol 27 (7) ◽  
pp. 356-361
Author(s):  
C. Dain ◽  
J.-C. Rozé ◽  
J. Caillon ◽  
C. Flamant ◽  
J.-B. Muller ◽  
...  

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